Clinical-Scientific – Quality Control Chemist

Company : Pioneer Data Systems

Country: United States

Location : Rocky Mount, North Carolina

Post: Tue, 30 May 2023 06:29:01 GMT

Expires: Tue, 27 Jun 2023 23:59:59 GMT

Apply Job : Apply Online

—————————— Job Description ——————————

Position Details:

Our client, a world-leading Pharmaceutical Company in Rocky Mount, NC is currently looking for a QC Chemist (HPLC, Empower 3) to join their expanding team.

Job Title: QC Chemist ( HPLC , Empower 3) / Pharma Industry

Duration: 6 months contract, extendable up to 36 months

Location: Rocky Mount, NC

Note:

The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.

You may participate in the company group medical insurance plan

Job Description:

Role Summary

The CQ Technical Data Reviewer reviews data from physical and dimensional testing of commodities, wet chemical techniques and instrumental analyses. Included in this review are visual evaluations, titrations, pH measurements, AA, HPLC, GC and UV/Vis among other analyses.

In addition to data review, this individual could be responsible for preparing solutions, performing analyses, as well as recording and processing data in accordance with DEA, FDA, and ICH guidelines, as needed.

Role Responsibilities

Functions as a dedicated data reviewer for the Chemical Quality Lab.

Prioritizes data review and testing with guidance from Data Coordinator or supervisor.

Assists in monitoring laboratory metrics associated with turnaround goals.

As needed, prepares solutions required for testing, performs analysis, records data according to cGMPs, performs calculations and enters results into LIMS system.

Provides support to assure lab safety and compliance -either through safe use of chemicals and/or the recognition of DEA, FDA, OSHA, and ICH compliance issues.

Basic Qualifications

Bachelor of Science in Life Science (e.g. Chemistry, Biology, Microbiology, etc.)

Minimum of 5 years of experience in a Quality Control or R&D laboratory and experience with a wide variety of analytical techniques (e.g., HPLC, GC, AA, UV-VIS, etc.) and biological techniques (e.g., BET, antibiotic potency, sterility, etc.).

Knowledge of cGMPs and regulations outside of the US.

Good communication, organization and computer skills are required.

Knowledge of LIMS, Empower, and Microsoft Office programs is desired.

Required Qualifications

Minimum of 1 year data review experience with minimum 5 yrs Lab Experience in pharmaceutical manufacturing environment.

Minimum of 4-5 years of experience reading and interpreting chromatographic data.

CP-MS Experience Preferred

Required Technical Experience:

HPLC basic experience (AA/ICP-MS)

Empower3 Experience

Chromatography Knowledge

cGMP

Day 2 Day:

HPLC

GC

AA/ICP-MS

Data Review

Notes:

True Experience is 3+ years

Onsite – will need to adhere to return to site policy

Assignments will be for 6-months with the possibility of extension up to 12-months

Minimum Education:

4 year Degree – Bachelor of Science in Life Science (e.g. Chemistry, Biology, Microbiology, etc.)